IHCRA Professional

3 - 7 years

4 - 7 Lacs

Posted:1 month ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

  • Assisting in the planning, initiation, and execution of clinical trial activities
  • Conducting site feasibility assessments and participating in site selection processes
  • Coordinating with investigative sites to ensure compliance with study protocols and regulatory requirements
  • Monitoring study progress and data collection activities to ensure quality and accuracy
  • Assisting in the preparation and review of study documentation and reports
Your profile
  • Bachelors degree in a relevant field, such as life sciences or healthcare
  • Previous experience in clinical research or a related field preferred
  • Strong organizational and communication skills
  • Ability to work independently and collaboratively in a fast-paced environment
  • Attention to detail and ability to prioritize tasks effectively

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St Albans Hertfordshire

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